27 results
Aortic Stenosis & Bicuspid Aortic Valve (AS)
 • Introduction & Pathophysiology
 • Classifications
 • Epidemiology
 •
Aortic Valve (AS ... Introduction & Pathophysiology ... Epidemiology • Clinical ... AorticValve #cardiology #peds
Nuchal Rigidity in Infantile Bacterial Meningitis

Flexion of the neck revealed nuchal rigidity. The patient was unable
back from the bed as ... #PhysicalExam #Clinical ... #Video #Peds #Pediatrics ... #neurology
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
the infant cries as ... Sign #Meningitis #Clinical ... PhysicalExam #Pediatrics #Peds ... #neurology
Amyotrophic Lateral Sclerosis (ALS) Summary
ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the clinical ... lateral sclerosis Pathophysiology ... cellular function Clinical ... signs to determine likelihood ... Lateral #Sclerosis #neurology
Bell's Palsy
Bell’s Palsy is a damage, acute weakness, or paralysis of the Facial nerve (7th CN),
unknown but its clinically ... infections such as ... #Bells #Palsy #neurology ... #anatomy #pathophysiology
Asymmetrical Tonic Neck Reflex (ATNR)

This primitive reflex found in newborn babies that normally vanishes around 4
Also known as the ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
Nuchal Rigidity in Infantile Bacterial Meningitis

Flexion of the neck revealed nuchal rigidity. The patient was unable
back from the bed as ... #PhysicalExam #Clinical ... #Video #Peds #Pediatrics ... #neurology
Aphasia - Pathophysiology and Clinical Findings
Broca's Aphasia - Expressive language impairment: non-Fluent
 - Sensory speech areas
Aphasia - Pathophysiology ... and Clinical Findings ... motor areas is also ... nearby areas is also ... Brocas #Wernickes #neurology
Causes of Neuromuscular Weakness
 • Spinal Cord: Demyelinating Disease (MS), Epidural abscess, Infarction, Syringomyelia, Tetanus, Transverse
Motor Nerves: ALS ... heavy metals), Critical ... Shellfish poisoning, Meds ... differential #diagnosis #neurology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... occur in utero as ... • This is also ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds